Transcript #00009868

Transcript name transcript variant 1
Gene name MAGEC3 (melanoma antigen family C, 3)
Chromosome X
Transcript - NCBI ID NM_138702.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_619647.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

101 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.33C>T r.(=) p.(=)
?/? c.41G>C r.(?) p.(Ser14Thr)
?/? c.66G>C r.(=) p.(=)
?/? c.87T>A r.(?) p.(Tyr29*)
?/? c.124-3T>C r.spl? p.?
?/? c.127C>T r.(?) p.(Arg43Trp)
?/? c.143A>T r.(?) p.(Asp48Val)
?/? c.200G>A r.(?) p.(Arg67Lys)
?/? c.240C>T r.(=) p.(=)
?/? c.249A>G r.(=) p.(=)
?/? c.258+16A>G r.(=) p.(=)
?/? c.259-44C>T r.(=) p.(=)
?/? c.259-15T>C r.(=) p.(=)
?/? c.279G>A r.(=) p.(=)
?/? c.307C>T r.(?) p.(His103Tyr)
?/? c.323C>T r.(?) p.(Pro108Leu)
?/? c.324G>A r.(=) p.(=)
?/? c.419A>T r.(?) p.(Asp140Val)
?/? c.426C>T r.(=) p.(=)
?/? c.447C>T r.(=) p.(=)
?/? c.448A>C r.(?) p.(Thr150Pro)
?/? c.453_469del r.(?) p.(Tyr152Cysfs*29)
?/? c.463T>C r.(?) p.(Ser155Pro)
?/? c.474C>T r.(=) p.(=)
?/? c.479G>A r.(?) p.(Ser160Asn)
?/? c.493T>A r.(?) p.(Leu165Met)
?/? c.495_497del r.(?) p.(Trp166del)
?/? c.509C>T r.(?) p.(Ala170Val)
?/? c.516-18T>C r.(=) p.(=)
?/? c.516-16C>T r.(=) p.(=)
?/? c.577C>T r.(?) p.(Gln193*)
?/? c.607G>A r.(?) p.(Glu203Lys)
?/? c.647A>G r.(?) p.(Asn216Ser)
?/? c.670A>G r.(?) p.(Met224Val)
?/? c.683A>G r.(?) p.(Lys228Arg)
?/? c.738C>T r.(=) p.(=)
?/? c.744T>G r.(?) p.(His248Gln)
?/? c.800A>G r.(?) p.(Glu267Gly)
?/? c.876del r.(?) p.(Glu293Argfs*7)
?/? c.909+23T>C r.(=) p.(=)
?/? c.910-24A>G r.(=) p.(=)
?/? c.919G>A r.(?) p.(Ala307Thr)
?/? c.933C>T r.(=) p.(=)
?/? c.935C>T r.(?) p.(Ala312Val)
?/? c.958C>T r.(=) p.(=)
?/? c.978T>A r.(=) p.(=)
?/? c.982G>A r.(?) p.(Ala328Thr)
?/? c.1024G>A r.(?) p.(Val342Ile)
?/? c.1037C>T r.(?) p.(Ala346Val)
?/? c.1040A>G r.(?) p.(Asn347Ser)
?/? c.1048+27G>A r.(=) p.(=)
?/? c.1048+32C>T r.(=) p.(=)
?/? c.1048+34C>A r.(=) p.(=)
?/? c.1049-29A>C r.(=) p.(=)
?/? c.1049-27G>A r.(=) p.(=)
?/? c.1061A>G r.(?) p.(His354Arg)
?/? c.1114A>G r.(?) p.(Lys372Glu)
?/? c.1123+52_1123+53insC r.(=) p.(=)
?/? c.1124-277C>A r.(=) p.(=)
?/? c.1124-276C>T r.(=) p.(=)
?/? c.1124-270C>G r.(=) p.(=)
?/? c.1124-205C>T r.(=) p.(=)
?/? c.1124-179G>A r.(=) p.(=)
?/? c.1124-156T>G r.(=) p.(=)
?/? c.1124-130_1124-125del r.(=) p.(=)
?/? c.1124-21C>T r.(=) p.(=)
?/? c.1162C>A r.(?) p.(Pro388Thr)
?/? c.1219C>G r.(?) p.(Pro407Ala)
?/? c.1223C>T r.(?) p.(Pro408Leu)
?/? c.1234C>T r.(?) p.(Pro412Ser)
?/? c.1272G>A r.(=) p.(=)
?/? c.1280G>A r.(?) p.(Arg427Gln)
?/? c.1282T>C r.(=) p.(=)
?/? c.1284G>A r.(=) p.(=)
?/? c.1298G>A r.(?) p.(Ser433Asn)
?/? c.1330G>A r.(?) p.(Ala444Thr)
?/? c.1332C>T r.(=) p.(=)
?/? c.1390G>T r.(?) p.(Val464Leu)
?/? c.1407C>T r.(=) p.(=)
?/? c.1418C>T r.(?) p.(Thr473Ile)
?/? c.1435A>G r.(?) p.(Lys479Glu)
?/? c.1456G>A r.(?) p.(Val486Ile)
?/? c.1464G>T r.(?) p.(Lys488Asn)
?/? c.1502C>T r.(?) p.(Ala501Val)
?/? c.1581C>T r.(=) p.(=)
?/? c.1599T>C r.(=) p.(=)
?/? c.1612A>T r.(?) p.(Ile538Phe)
?/? c.1666A>T r.(?) p.(Ile556Phe)
?/? c.1699G>T r.(?) p.(Val567Phe)
?/? c.1702A>T r.(?) p.(Ile568Phe)
?/? c.1727G>A r.(?) p.(Gly576Glu)
?/? c.1728+46C>G r.(=) p.(=)
?/? c.1728+48G>T r.(=) p.(=)
?/? c.1728+54T>C r.(=) p.(=)
?/? c.1728+60T>C r.(=) p.(=)
?/? c.1729-34C>G r.(=) p.(=)
?/? c.1748G>C r.(?) p.(Arg583Thr)
?/? c.1813A>G r.(?) p.(Met605Val)
?/? c.1828G>C r.(?) p.(Asp610His)
?/? c.1829A>G r.(?) p.(Asp610Gly)
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